Hanhart Syndrome: An autosomal recessive disorder due to a deficiency in the body of the tyrosine amino transferase enzyme. More detailed information about the symptoms, causes, and treatments of Hanhart Syndrome is available below.
See full list of 9 symptoms of Hanhart Syndrome
Read more about complications of Hanhart Syndrome.
Read more about causes of Hanhart Syndrome.
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Read more about Misdiagnosis and Hanhart Syndrome
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Types of Hanhart Syndrome
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Hanhart Syndrome is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Hanhart Syndrome, or a subtype of Hanhart Syndrome,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Ophanet, a consortium of European partners,
currently defines a condition rare when it affects 1 person per 2,000.
They list Hanhart Syndrome as a "rare disease".
Source - Orphanet
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